A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031639



Internal ID88806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37441881..37765327hg38UCSC Ensembl
chr10:37730809..38054255hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38323447
hg19323447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489960
Supporting Variants
Samples
Known GenesMTRNR2L7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031639
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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